Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr9:33625262-33625303 | Rare:14 | ||||
chr9:33923023-33923234 | Rare:73 | ||||
chr9:33982658-33982865 | Rare:45 | ||||
chr9:34412622-34412978 | Common:2; Rare:54 | ||||
chr9:34432275-34432447 | Rare:16 | ||||
chr9:34635768-34636139 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
chr9:34996817-34997147 | Common:1; Rare:74 | ||||
chr9:35086032-35086073 | Rare:5 | ||||
chr9:35341753-35341852 | Rare:18 | ||||
chr9:35520416-35520688 | Rare:40 | ||||
chr9:35688997-35689291 | Rare:75; Clinvar:1; Clinvar (benign):1 | ||||
chr9:35706768-35707256 | Common:2; Rare:137 | ||||
chr9:35718825-35719157 | Rare:89 | ||||
chr9:35725237-35725637 | Common:1; Rare:88 | ||||
chr9:35727744-35727947 | Common:1; Rare:43 |